Symbol Name ID |
Notch1
notch 1 MGI:97363 |
Darker colors indicate more annotations |
Human Phenotypes | Portal vein thrombosis |
Portal hypertension |
Cirrhosis |
Congenital hepatic fibrosis |
Disease(s) Associated with NOTCH1 | ||||
Adams-Oliver syndrome |
Mouse Phenotypes | dilated liver sinusoidal space |
increased liver weight |
chronic liver inflammation |
abnormal liver morphology |
abnormal hepatic cord morphology |
abnormal liver parenchyma morphology |
abnormal liver lobule morphology |
hepatic steatosis |
pale liver |
increased cholangiocarcinoma incidence |
|
Availability | Mouse Genotype | ||||||||||
Albtm1(cre/ERT2)Mtz/Alb+ Gt(ROSA)26Sortm1(Notch1)Dam/Gt(ROSA)26Sor+ (conditional) |
|||||||||||
Gt(ROSA)26Sortm1(Notch1)Dam/Gt(ROSA)26Sor+ Tg(Adipoq-cre)1Evdr/0 (conditional) |
|||||||||||
Notch1tm2Rko/Notch1tm3(cre)Rko (conditional) |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/30/2024 MGI 6.23 |
|
|